Treatment of gum disease by periodontal surgery
- Conditions
- Health Condition 1: null- Chronic periodontitis patients
- Registration Number
- CTRI/2014/02/004405
- Lead Sponsor
- Saveetha Dental College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 32
1.Subjects within the age group of 30 years to 50 years.
2.Subjects with Chronic Periodontitis ( On basis of 1999 consensus classification of periodontal disease)
3.Presence of inter-proximal IBDs >= 2mm deep (distance between alveolar crest and base of the defect on IOPA)
4.Presence of inter-proximal probing depth(PD) >= 5mm following phase I therapy (SRP)
5.Systemically healthy subjects with no debilitating conditions.
1.Subjects with history of periodontal surgical treatment within the last six months.
2.Former / current smokers.
3.Immuno-comprimised subjects.
4.Subjects having unacceptable oral hygiene (PI >1.5) after re-evaluation of phase I therapy.
5.Pregnant and lactating mothers.
6.Subjects on antibiotic therapy within the last six months.
7.Subjects on treatment with steroids.
8.Subjects with non-vital teeth, teeth with furcation defects or teeth with mobility >= Grade II and teeth with endodontic-periodontal involvement.
9.Acute abscesses of periodontium.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Plaque Index(PI)- (Silness and Loe index) <br/ ><br>2.Sulcus Bleeding Index(m SBI) <br/ ><br>3.Gingival Marginal Level (GML) <br/ ><br>4.Probing Pocket Depth (PPD) <br/ ><br>5.Clinical attachment loss (CAL <br/ ><br>6. Defect depth <br/ ><br>Timepoint: All the outcomes to be assessed at the end of 3 months, 6 months and 9 months post-operatively
- Secondary Outcome Measures
Name Time Method Defect depthTimepoint: Baseline and 9 months